Zdrowie i gospodarka · 26/06/2019
FDA Requests Public Comment on Proposed Collection of Information for Clinical Laboratory Improvement Amendments Categorization
The Food and Drug Administration is seeking public input on its proposed procedures for categorizing certain in vitro diagnostic tests under the Clinical Laboratory Improvement Amendments of 1988, as required by the Paperwork Reduction Act of 1995.
Source: Federal Register — Food and Drug AdministrationOpen original release →